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大鼠心脏中钙调蛋白依赖性蛋白激酶II δ亚基同工型表达的发育变化

Developmental changes in isoform expression of Ca2+/calmodulin-dependent protein kinase II delta-subunit in rat heart.

作者信息

Hagemann D, Hoch B, Krause E G, Karczewski P

机构信息

Max Delbrück Center for Molecular Medicine, Berlin-Buch, Germany.

出版信息

J Cell Biochem. 1999 Aug 1;74(2):202-10.

Abstract

In the heart, Ca2+/calmodulin-dependent protein kinase II is critically involved in the regulation of Ca2+ homeostasis. Previously the predominant expression of a subclass of Ca2+/calmodulin-dependent protein kinase II delta-subunit, containing a second variable domain, was demonstrated in cardiac tissue. Here we report on the expression pattern of the non-neuronal members of this delta-subunit subclass, delta 2, delta 3, delta 4, and delta 9 in the developing heart of the rat. By semiquantitative RT-PCR isoform delta 3 was shown to be typically expressed in the heart, whereas delta 4 was expressed in skeletal muscle of adult rat. From embryonic day 14 up to the adult state of rat ventricular muscle, amounts of delta 9 transcripts remained unchanged, transcript levels of isoforms delta 2 and delta 3 were significantly increased, whereas level of delta 4 transcript was significantly decreased. Immunoblotting, using an antibody recognizing specifically those delta-isoforms containing the second variable domain, revealed three separated protein signals at about 59 kDa, 58 kDa, and 56 kDa. The immunoreaction at about 59 kDa, corresponding to the predicted molecular mass of delta 4, was dramatically diminished, whereas a significant increase in the signal at about 58 kDa was assumed to represent an increase in isoform delta 3. The protein signal at about 56 kDa, close to the predicted molecular mass of isoform delta 2, was high in the embryonic heart and significantly decreased after birth. Our data suggest the predominant expression of isoform delta 2 in the embryonic heart, establish delta 3 to be the typical isoform in the adult heart and define the skeletal muscle form delta 4 to be characteristic for fetal and neonatal stages of the heart.

摘要

在心脏中,钙/钙调蛋白依赖性蛋白激酶II在钙稳态调节中起关键作用。此前已证实在心脏组织中主要表达一类含有第二个可变结构域的钙/钙调蛋白依赖性蛋白激酶IIδ亚基。在此,我们报告该δ亚基子类的非神经元成员δ2、δ3、δ4和δ9在大鼠发育心脏中的表达模式。通过半定量逆转录聚合酶链反应(RT-PCR)表明,δ3亚型在心脏中典型表达,而δ4在成年大鼠骨骼肌中表达。从胚胎第14天到大鼠心室肌的成年状态,δ9转录本的量保持不变,δ2和δ3亚型的转录水平显著增加,而δ4转录本水平显著降低。使用特异性识别那些含有第二个可变结构域的δ亚型的抗体进行免疫印迹分析,显示在约59 kDa、58 kDa和56 kDa处有三个分离的蛋白信号。约59 kDa处的免疫反应对应于δ4的预测分子量,显著减弱,而约58 kDa处信号的显著增加被认为代表δ3亚型的增加。约56 kDa处的蛋白信号接近δ2亚型的预测分子量,在胚胎心脏中较高,出生后显著降低。我们的数据表明δ2亚型在胚胎心脏中占主导表达,确定δ3是成年心脏中的典型亚型,并确定骨骼肌形式的δ4是心脏胎儿和新生儿阶段的特征。

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